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Peter Krieg

Showing results (21-30 of 26) with videos related to

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The Biochemical Journal|March 7, 2008
Adipocyte differentiation of 3T3-L1 preadipocytes is dependent on lipoxygenase activity during the initial stages of the differentiation processLise Madsen, Rasmus K Petersen, Morten B Sørensen, et al.
The Journal of Investigative Dermatology|January 10, 2009
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12BKatja-Martina Eckl, Silvia de Juanes, Janine Kurtenbach, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 8, 2023
Impaired Brain Growth in Myelin Oligodendrocyte Glycoprotein Antibody-Associated Acute Disseminated EncephalomyelitisFrederik Bartels, Birgit Baumgartner, Annette Aigner, et al.
The Journal of Investigative Dermatology|November 25, 2018
Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid EnvelopeDebra Crumrine, Denis Khnykin, Peter Krieg, et al.
Journal of Neuroinflammation|September 5, 2020
Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patientsSven Jarius, Christian Lechner, Eva M Wendel, et al.
American Journal of Human Genetics|May 17, 2023
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorderDmitrijs Rots, Taryn E Jakub, Crystal Keung, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
The Biochemical Journal|March 7, 2008
Adipocyte differentiation of 3T3-L1 preadipocytes is dependent on lipoxygenase activity during the initial stages of the differentiation processLise Madsen, Rasmus K Petersen, Morten B Sørensen, et al.
The Journal of Investigative Dermatology|January 10, 2009
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12BKatja-Martina Eckl, Silvia de Juanes, Janine Kurtenbach, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 8, 2023
Impaired Brain Growth in Myelin Oligodendrocyte Glycoprotein Antibody-Associated Acute Disseminated EncephalomyelitisFrederik Bartels, Birgit Baumgartner, Annette Aigner, et al.
The Journal of Investigative Dermatology|November 25, 2018
Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid EnvelopeDebra Crumrine, Denis Khnykin, Peter Krieg, et al.
Journal of Neuroinflammation|September 5, 2020
Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patientsSven Jarius, Christian Lechner, Eva M Wendel, et al.
American Journal of Human Genetics|May 17, 2023
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorderDmitrijs Rots, Taryn E Jakub, Crystal Keung, et al.
Pageof 3